A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148708



Internal ID15855757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104257096..104335962hg38UCSC Ensembl
Innerchr14:104723433..104802299hg19UCSC Ensembl
Innerchr14:103793186..103873344hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3878867
hg1978867
hg1880159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566039
Supporting Variants
Samples1782681313_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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